{{Rsnum
|rsid=7849530
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|position=92165453
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 78.8 | 20.4 | 0.9
| HCB | 75.2 | 22.6 | 2.2
| JPT | 93.8 | 6.2 | 0.0
| YRI | 40.1 | 47.6 | 12.2
| ASW | 45.6 | 45.6 | 8.8
| CHB | 75.2 | 22.6 | 2.2
| CHD | 83.5 | 14.7 | 1.8
| GIH | 53.5 | 38.6 | 7.9
| LWK | 29.1 | 53.6 | 17.3
| MEX | 75.9 | 22.4 | 1.7
| MKK | 50.0 | 41.0 | 9.0
| TSI | 80.4 | 18.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=25140149
|Title=Genetic variation modifies risk for neurodegeneration based on biomarker status
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}